IndraLab
Statements
reach
"Its increased expression correlates with prostate cancer progression to castration resistant disease [XREF_BIBR] and it is essential for EGF promoted cell migration and invasion, as well as for EMT markers expression [XREF_BIBR], AKT and GSK3beta phosphorylation induced by EGF, and consequently for beta-catenin stabilization [XREF_BIBR]."
sparser
"Since ErbB2-4 receptor phosphorylation is required for substrate interaction and activation through tyrosine phosphorylation [ xref , xref ], a reduction in ErbB receptor activation also resulted in a corresponding decrease in EGF-dependent phosphorylation (activation) of Akt, NFκB, and GSK-3β."
sparser
"For GSK3β, the effects were less clear—for ARPE-19 cells, there was a tendency for less phosphorylation of GSK3β ( xref ), but this was not the case for MDA-MB-231 cells ( xref ); neither cell line demonstrated a significant decrease in EGF-stimulated GSK3β phosphorylation upon LCLAT1 silencing."
reach
"Since ErbB2-4 receptor phosphorylation is required for substrate interaction and activation through tyrosine phosphorylation [XREF_BIBR, XREF_BIBR], a reduction in ErbB receptor activation also resulted in a corresponding decrease in EGF dependent phosphorylation (activation) of Akt, NFkappaB, and GSK-3beta."
reach
"In RKTG-null mouse embryonic fibroblasts, lypophosphatidic acid (LPA), but not EGF (epidermal growth factor), could stimulate hyperphosphorylation of AKT and GSK3beta, accompanied by increases in phosphorylation of p53 at Ser15 and accumulation of p53, as well as its target genes p21 and p16."
sparser
"The previous researches prompt that HSP27 can regulate EGF-induced AKT and GSK3b phosphorylation, inhibit β-catenin ubiquitinoylation and degradation, and then prevent combination of β-catenin nuclear translocation with Slug promoter, thus promoting EMT to drive tumor development ( xref )."
sparser
"Its increased expression correlates with prostate cancer progression to castration-resistant disease [ xref ] and it is essential for EGF-promoted cell migration and invasion, as well as for EMT markers expression [ xref ], AKT and GSK3β phosphorylation induced by EGF, and consequently for β-catenin stabilization [ xref ]."
reach
"The previous researches prompt that HSP27 can regulate EGF-induced AKT and GSK3b phosphorylation, inhibit β-catenin ubiquitinoylation and degradation, and then prevent combination of β-catenin nuclear translocation with Slug promoter, thus promoting EMT to drive tumor development (20)."